Pediatric cholesteatoma and variants in the gene encoding connexin 26
Author:
Publisher
Wiley
Subject
Otorhinolaryngology
Reference22 articles.
1. Human Connexins in Skin Development and Skin Disorders
2. Expression of the gap junction proteins connexin 26 and connexin 43 in human middle ear cholesteatoma;Choung;Acta Otolaryngol,2006
3. A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families;Maestrini;Hum Mol Genet,1999
4. Expanding the phenotypic spectrum of Cx26 disorders: Bart-Pumphrey syndrome is caused by a novel missense mutation in GJB2;Richard;J Invest Dermatol,2004
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